Structure of a self-assembled hydrogen-bonded ‘living’ main chain liquid crystalline polymer
✍ Scribed by Chaobin He; Athene M. Donald; Anselm C. Griffin; Tom Waigh; Alan H. Windle
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 209 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-6266
No coin nor oath required. For personal study only.
✦ Synopsis
A main chain hydrogen-bonded liquid crystalline polymer was formed by melt mixing two complementary components, A and B, which in their individual states do not exhibit liquid crystallinity. The structure of the polymer and the thermal stability of its mesophase were studied using synchrotron radiation SAXS/WAXS/DSC at Daresbury (UK) and by variable temperature Fourier transform infrared. The chain extension, or ''polymerization'' process, was accelerated at the point when the polymer formed a liquid crystalline phase upon cooling from the isotropic melt. The polymer has an aabb chain structure and forms a smectic layer with a length of the A-B repeating unit. The hydrogen-bonded main chain polymer studied here is a monotropic liquid crystal. Above 150ЊC, it exhibits kinetic stabilization of its monotropic smectic phase.
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## Abstract Physical phenomena such as glass transition temperatures, melting points, and relaxational behavior have been determined for a wide range of thermotropic liquid crystalline polymers (TLCPs) and polycarbonate (PC). Damping intensities of rigid TLCPs during glass transition are greater th